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用于细胞冷冻保存的基于明胶的液滴弹。

The gelatin-based liquid marbles for cell cryopreservation.

作者信息

Liu Min, Chen Changhong, Yu Jiajun, Zhang Haitao, Liang Lei, Guo Bingyan, Qiu Yuwei, Yao Fanglian, Zhang Hong, Li Junjie

机构信息

Department of Polymer Science, School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, China.

Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300350, China.

出版信息

Mater Today Bio. 2022 Oct 31;17:100477. doi: 10.1016/j.mtbio.2022.100477. eCollection 2022 Dec 15.

DOI:10.1016/j.mtbio.2022.100477
PMID:36388455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9641251/
Abstract

As an alternative and a straightforward cryopreservation biotechnological tool, liquid marble provides a promising cryopreservation approach. Currently, effective cell preservation mainly based on the addition of dimethyl sulfoxide (DMSO) and fetal bovine serum (FBS). As state-of-the-art cryoprotectant (CPA), DMSO, has intrinsic toxicity, which is the bottleneck of its widespread application. The complex compositions of FBS have the potential risks of pathogenic microorganism contamination. However, efficient cell cryopreservation using liquid marbles, a platform independent of DMSO and FBS, has not been well investigated yet. Herein, we explore the cryoprotection role of liquid marbles based on gelatin solution. Gelatin has a superior biocompatibility, which DMSO is incomparable. During a freeze-thaw cycle, gelatin produces negligible osmotic pressure, and has high ice recrystallization inhibition (IRI) activity to induce the formation of smaller and smooth ice crystals. Moreover, the specific structure of liquid marble also provides favorable supports for cell survival. The cryopreservation efficiency of mouse fibroblasts cells L929 via the gelatin-based liquid marble was as high as 90%, and the recovered cells could maintain their normal functionalities. This work opens a new window of opportunity for non-toxic and efficient cryopreservation of liquid marbles without the need of DMSO and FBS addition.

摘要

作为一种替代性的直接冷冻保存生物技术工具,液滴弹提供了一种很有前景的冷冻保存方法。目前,有效的细胞保存主要基于添加二甲基亚砜(DMSO)和胎牛血清(FBS)。作为最先进的冷冻保护剂(CPA),DMSO具有内在毒性,这是其广泛应用的瓶颈。FBS的复杂成分存在病原微生物污染的潜在风险。然而,使用独立于DMSO和FBS的平台——液滴弹进行高效细胞冷冻保存的研究尚未充分开展。在此,我们探索基于明胶溶液的液滴弹的冷冻保护作用。明胶具有优异的生物相容性,这是DMSO无法比拟的。在冻融循环过程中,明胶产生的渗透压可忽略不计,并且具有高抗冰重结晶(IRI)活性,可诱导形成更小、更光滑的冰晶。此外,液滴弹的特殊结构也为细胞存活提供了有利支持。通过基于明胶的液滴弹对小鼠成纤维细胞L929进行冷冻保存的效率高达90%,复苏后的细胞能够保持其正常功能。这项工作为无需添加DMSO和FBS的无毒高效液滴弹冷冻保存打开了新的机遇之窗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/aeacf1d14af3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/f52c6551d285/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/dc2ff598d6ef/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/eccfc740ed88/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/c0a80b18e298/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/6e6712d5fa9b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/aeacf1d14af3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/f52c6551d285/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/dc2ff598d6ef/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/eccfc740ed88/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/c0a80b18e298/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/6e6712d5fa9b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4b/9641251/aeacf1d14af3/gr6.jpg

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